Sanders-Haigh L, Anderson W F, Francke U
Nature. 1980 Feb 14;283(5748):683-6. doi: 10.1038/283683a0.
Investigations on the regulation of human globin gene expression are assisted by a knowledge of the chromosomal location of the globin genes. Previous studies have mapped the alpha-globin locus to human chromosome (HC) 16, and have shown that the human globin gene complex gamma-delta-beta co-segregates with lactate dehydrogenase A (LDH-A) and the presence of HC 11 in somatic cell hybrids. Radioactively labelled globin complementary DNA (cDNA) probes were used in molecular hybridisation experiments to determine the chromosomal locations of the alpha- and beta-globin genes. When human x rodent somatic cell hybrids are used which contain well-defined parts of human chromosomes, direct mapping of genes of chromosomal regions or single bands is possible. We have regionally localised the human beta-globin gene using two sets of hybrid cell lines: (1) Chinese hamster x human hybrid cells containing the HC 11 long arm or both the short and long arms and (2) mouse x human hybrids containing only the HC 11 short arm. The techniques of liquid molecular hybridisation and Southern blotting with 32P-labelled human beta-globin cDNA (from plasmid JW102) have been used to localise the beta-globin gene sequence to region 11p11 leads to 11p15. Similar results were reported recently by Jeffreys et al.
对人类珠蛋白基因表达调控的研究借助于对珠蛋白基因染色体定位的了解。先前的研究已将α-珠蛋白基因座定位于人类染色体(HC)16,并表明人类珠蛋白基因复合体γ-δ-β与乳酸脱氢酶A(LDH-A)以及在体细胞杂种中存在的HC 11共分离。放射性标记的珠蛋白互补DNA(cDNA)探针用于分子杂交实验,以确定α-和β-珠蛋白基因的染色体位置。当使用含有明确人类染色体部分的人×啮齿动物体细胞杂种时,对染色体区域或单个条带的基因进行直接定位是可能的。我们使用两组杂交细胞系对人类β-珠蛋白基因进行了区域定位:(1)含有HC 11长臂或短臂和长臂的中国仓鼠×人类杂交细胞,以及(2)仅含有HC 11短臂的小鼠×人类杂种。已使用液体分子杂交技术和用32P标记的人类β-珠蛋白cDNA(来自质粒JW102)进行的Southern印迹法,将β-珠蛋白基因序列定位到11p11至11p15区域。Jeffreys等人最近报道了类似的结果。